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Data / Medical devices / Thailand / Avita Corp (thailand) Co., Ltd.

Avita Corp (thailand) Co., Ltd.: FDA-registered device maker in Chonburi Chon Buri, Thailand, 8 510(k) clearances

Avita Corp (thailand) Co., Ltd. is registered with the FDA (registration 3042156936) in Chonburi Chon Buri, Thailand. It lists 9 device types. The FDA files 8 510(k) clearances under its listings, the newest dated December 31, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3042156936
Address
No. 8/9 Moo 4, Bangnang-Laemkhae Road Bangnang Sub-District, Panthong District, Chonburi Chon Buri, Thailand, 20160
Owner or operator
AViTA CORP (THAILAND) CO., LTD. (10094377)
Roles
Manufacturer
First device listed
November 26, 2025
Registered through
2026
Brand names listed
AViTA BPM 22 Wrist Type Blood Pressure Monitor, AViTA BPM Ix Series Wrist Type Blood Pressure Monitor, AViTA Blood Pressure Monitor BPM82, AViTA Blood Pressure Monitor BPM92, AViTA NE10, AViTA NE20, AViTA NS18, AViTA NT17 and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 31, 2024K241852Nasal Aspirator (NS 13)BTASubstantially EquivalentAvita Corporationaccessdata.fda.gov
October 22, 2024K242193Arm Type Blood Pressure Monitor (BPM82)DXNSubstantially EquivalentAvita Corporationaccessdata.fda.gov
May 20, 2024K223399AViTA Pulse OximeterDQASubstantially EquivalentAvita Corporationaccessdata.fda.gov
July 23, 2018K181242Braun BNT400 No Touch + Forehead ThermometerFLLSubstantially EquivalentKaz USA, Inc., A Helen of Troy Companyaccessdata.fda.gov
April 19, 2018K172427AViTA Radar Thermo NT16 Series IR ThermometerFLLSubstantially EquivalentAvita Corporationaccessdata.fda.gov
March 3, 2011K102554AVITA SCANEO IR THERMOMETER MODEL TS4X SERIESFLLSubstantially EquivalentAvita Corporationaccessdata.fda.gov
December 16, 2010K102624AVITA WRIST TYPE BLOOD PRESSURE MONITORDXNSubstantially EquivalentAvita Corporationaccessdata.fda.gov
May 26, 2010K090379AVITA NASAL ASPIRATOR, MODEL, NS1 SERIESBTASubstantially EquivalentAvita Corporationaccessdata.fda.gov

Compare with other makers

Updated December 31, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.